Thompson J, Saier M H
J Bacteriol. 1981 Jun;146(3):885-94. doi: 10.1128/jb.146.3.885-894.1981.
Starved cells of Streptococcus lactis ML3 (grown previously on galactose, lactose, or maltose) accumulated methyl-beta-D-thiogalactopyranoside (TMG) by the lactose:phosphotransferase system. More than 98% of accumulated sugar was present as a phosphorylated derivative, TMG-6-phosphate (TMG-6P). When a phosphotransferase system sugar (glucose, mannose, 2-deoxyglucose, or lactose) was added to the medium simultaneously with TMG, the beta-galactoside was excluded from the cells. Galactose enhanced the accumulation of TMG-6P. Glucose, mannose, lactose, or maltose plus arginine, was added to a suspension of TMG-6P-loaded cells of S. lactis ML3, elicited rapid expulsion of intracellular solute. The material recovered in the medium was exclusively free TMG. Expulsion of galactoside required both entry and metabolism of an appropriate sugar, and intracellular dephosphorylation of TMG-6P preceded efflux of TMG. The rate of dephosphorylation of TMG-6P by permeabilized cells was increased two-to threefold by adenosine 5'-triphosphate but was strongly inhibited by fluoride. S. lactis ML3 (DGr) was derived from S. lactis ML3 by positive selection for resistance to 2-deoxy-D-glucose and was defective in the enzyme IIMan component of the glucose:phosphotransferase system. Neither glucose nor mannose excluded TMG from cells of S. lactic ML3 (DGr), and these two sugars failed to elicit TMG expulsion from preloaded cells of the mutant strain. Accumulation of TMG-6P by S. lactis ML3 can be regulation by two independent mechanisms whose activities promote exclusion or expulsion of galactoside from the cell.
乳酸链球菌ML3的饥饿细胞(先前在半乳糖、乳糖或麦芽糖上生长)通过乳糖磷酸转移酶系统积累甲基-β-D-硫代半乳糖苷(TMG)。积累的糖中超过98%以磷酸化衍生物TMG-6-磷酸(TMG-6P)的形式存在。当磷酸转移酶系统的糖(葡萄糖、甘露糖、2-脱氧葡萄糖或乳糖)与TMG同时添加到培养基中时,β-半乳糖苷被排除在细胞外。半乳糖增强了TMG-6P的积累。将葡萄糖、甘露糖、乳糖或麦芽糖加精氨酸添加到负载TMG-6P的乳酸链球菌ML3细胞悬液中,会引起细胞内溶质的快速排出。培养基中回收的物质仅为游离TMG。半乳糖苷的排出需要合适糖的进入和代谢,并且TMG-6P的细胞内去磷酸化先于TMG的流出。通透细胞对TMG-6P的去磷酸化速率被三磷酸腺苷提高了两到三倍,但被氟化物强烈抑制。乳酸链球菌ML3(DGr)是通过对2-脱氧-D-葡萄糖抗性的正向选择从乳酸链球菌ML3衍生而来,并且在葡萄糖磷酸转移酶系统的酶IIMan组分中存在缺陷。葡萄糖和甘露糖都不能将TMG排除在乳酸链球菌ML3(DGr)细胞外,并且这两种糖不能从突变菌株的预负载细胞中引发TMG排出。乳酸链球菌ML3对TMG-6P的积累可由两种独立机制调节,其活性促进半乳糖苷从细胞中被排除或排出。